ASPARAGINE SYNTHETASE DEFICIENCY
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(OMIM:615574)
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CEREBROOCULOFACIOSKELETAL SYNDROME 4
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(OMIM:610758)
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MICROCEPHALY 2, PRIMARY, AUTOSOMAL RECESSIVE, WITH OR WITHOUT CORTICALMALFORMATIONS
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(OMIM:604317)
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MICROCEPHALY 3, PRIMARY, AUTOSOMAL RECESSIVE
|
(OMIM:604804)
|
MICROCEPHALY 9, PRIMARY, AUTOSOMAL RECESSIVE
|
(OMIM:614852)
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Microcephaly - seizures - developmental delay
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(Orphanet:228418)
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Microcephaly-cerebellar hypoplasia-cardiac conduction defect syndrome
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(Orphanet:329332)
|
Microlissencephaly
|
(Orphanet:1083)
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Primary microcephaly-epilepsy-permanent neonatal diabetes syndrome
|
(Orphanet:306558)
|
RETT SYNDROME, CONGENITAL VARIANT
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(OMIM:613454)
|
VAN MALDERGEM SYNDROME 1
|
(OMIM:601390)
|